Annotation Detail
Information
- Associated Genes
- NF1
- Associated Variants
-
NF1 p.Thr780Lys (p.T780K)
(
ENST00000691014.1,
ENST00000356175.7,
ENST00000358273.9,
ENST00000696138.1 )
NF1 p.Thr780Lys (p.T780K) ( ENST00000356175.7, ENST00000358273.9, ENST00000691014.1, ENST00000696138.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001042492.3(NF1):c.2339C>A (p.Thr780Lys) AND not provided
- ClinVar Allele ID
- 79207
- ClinVar RefSeq Alternation Syntax
- NM_001042492.3:c.2339C>A
- ClinVar RefSeq Alternation Syntax
- NM_000267.3:c.2339C>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2017-12-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000059168
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- not provided
Drugs